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ProThera, Inc. dba SFI USA

2 recalls on record

This page lists all FDA food recalls initiated by ProThera, Inc. dba SFI USA. Data is sourced directly from the FDA enforcement database and updated weekly. Class I recalls indicate the most serious health risk.

Small quantity of product labeled as Melatonin Lozenge Formula were filled with L-Theanine.
Class III2019-01-17#F-1101-2019
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
Class II2018-12-13#F-1186-2019

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ListeriaSalmonellaE. coliUndeclared allergensPeanutUndeclared milkWheat / glutenForeign materialMetal contaminationGlass contaminationPlastic contaminationMold / spoilageLabeling errorsHepatitis ANorovirus